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Pandit Govind Ballabh Pant Memorial Lecture: II

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Similar<br />

Distinct<br />

Distinct<br />

ECOTYPE<br />

(ecological<br />

races)<br />

The same The same<br />

entity<br />

Genetic species only (Example:<br />

autoploidy; certain kinds of<br />

chromosomal repattering<br />

Fig. 11. Relationship between systematics, genetics and ecology<br />

Behind such a common genetic and ecological thread, there are the specific<br />

attributes of genetic diversity, life history traits, population dynamics including its<br />

genetic architecture which equips a species to interact with other species and<br />

environment. Genetic diversity also equips a species at the molecular level to<br />

generate new variation through the processes of mutation, recombination and<br />

natural selection, leading to elimination of some and selection of others. Thus a<br />

phenotype is the result of interaction between genotype and environment. The<br />

phenotypic characteristic of an individual are coded into the genes of a taxon which<br />

determines whether it is going to be miniscule virus or an amoebae, or a giant like<br />

squoia, elephant or a whale. Today’s biodiversity is, therefore, the result of mutation,<br />

recombination and natural selection having taken place during the last 3 billion<br />

years. Life began with a DNA molecule having properties of self-replication, mutation<br />

and recombination. Genetic diversity is, therefore a prerequisite for all biological<br />

evolution leading to diversity (see also Solbrig, 1991). Biodiversity can be reduced<br />

both by habitat destruction leading to failure of populations to recover from mortality<br />

caused by habitat disturbances, and also by competitive exclusion thus there is<br />

interaction between competitive exclusion and mortality due to habitat disturbance.<br />

According to Huston (1991), when these two opposing trends are balanced, there is<br />

maximum biodiversity at intermediate disturbance level.<br />

Intraspecific genetic diversity is the fundamental building block of maintaining<br />

biodiversity. The natural selection acts on this, and populations are refined to<br />

function as interacting units within communities and ecosystems. The genetic<br />

consequence of habitat fragmentation leads to restrictions in gene flow and may be,<br />

in course time, to genetic differentiation. The particular life form of a species is also<br />

the consequence of selection. Thus, there are pine forests in the Himalaya. These<br />

are essentially large populations of big individuals with long life and good seed<br />

dispersal. Such populations have high productivity and live in low habitat<br />

disturbances. Conversely low productivity and high habitat distrubances. Destruction<br />

occurs due to abiotic causes (like extreme climatic conditions, fire, floods, etc) or<br />

biotic causes; (like parasitism, disease, predation, herbivory etc.). These lead to a<br />

competitive advantage for smaller populations, of small individuals with short life<br />

cycles. There are many such correlations (Stebbins, 1950;Grant, 1958, Gadgil and<br />

Solbrig 1972). The measurement of diversity can be at the allelic level within<br />

individuals or species, or at the level of gene pool on a population. This diversity can<br />

be studied through RFLP and RAPD. Next follows species richness in a community<br />

44

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